Literature DB >> 25044433

Laccase-mediator system for alcohol oxidation to carbonyls or carboxylic acids: toward a sustainable synthesis of profens.

Paola Galletti1, Matteo Pori, Federica Funiciello, Roberto Soldati, Alberto Ballardini, Daria Giacomini.   

Abstract

By combining two green and efficient catalysts, such as the commercially available enzyme laccase from Trametes versicolor and the stable free radical 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO), the oxidation in water of some primary alcohols to the corresponding carboxylic acids or aldehydes and of selected secondary alcohols to ketones can be accomplished. The range of applicability of bio-oxidation is widened by applying the optimized protocol to the oxidation of enantiomerically pure 2-arylpropanols (profenols) into the corresponding 2-arylpropionic acids (profens), in high yields and with complete retention of configuration.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alcohols; drug design; enzyme catalysis; oxidation; selectivity

Mesh:

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Year:  2014        PMID: 25044433     DOI: 10.1002/cssc.201402136

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  3 in total

1.  Sodium periodate/TEMPO as a selective and efficient system for amine oxidation.

Authors:  P Galletti; G Martelli; G Prandini; C Colucci; D Giacomini
Journal:  RSC Adv       Date:  2018-03-07       Impact factor: 4.036

2.  Efficient and sustainable laccase-catalyzed iodination of p-substituted phenols using KI as iodine source and aerial O2 as oxidant.

Authors:  Mark Sdahl; Jürgen Conrad; Christina Braunberger; Uwe Beifuss
Journal:  RSC Adv       Date:  2019-06-21       Impact factor: 4.036

3.  Stable ABTS Immobilized in the MIL-100(Fe) Metal-Organic Framework as an Efficient Mediator for Laccase-Catalyzed Decolorization.

Authors:  Youxun Liu; Yuanyuan Geng; Mingyang Yan; Juan Huang
Journal:  Molecules       Date:  2017-06-02       Impact factor: 4.411

  3 in total

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